(Q47947643)
Statements
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Autosomal dominant transmission of congenital hypothyroidism, neonatal respiratory distress, and ataxia caused by a mutation of NKX2-1. (English)
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Daniel A Doyle
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Iris Gonzalez
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Becky Thomas
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Mena Scavina
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1 August 2004
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145
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190-193
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2
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Identifiers
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